US5468791A - Primers containing zircoaluminate coupling agents for improved adhesion - Google Patents
Primers containing zircoaluminate coupling agents for improved adhesion Download PDFInfo
- Publication number
- US5468791A US5468791A US08/343,866 US34386694A US5468791A US 5468791 A US5468791 A US 5468791A US 34386694 A US34386694 A US 34386694A US 5468791 A US5468791 A US 5468791A
- Authority
- US
- United States
- Prior art keywords
- weight
- binder
- polyester
- primer
- primer composition
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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- 239000000049 pigment Substances 0.000 claims abstract description 13
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- 150000004072 triols Chemical class 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000012463 white pigment Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- LRXTYHSAJDENHV-UHFFFAOYSA-H zinc phosphate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LRXTYHSAJDENHV-UHFFFAOYSA-H 0.000 description 1
- 229910000165 zinc phosphate Inorganic materials 0.000 description 1
- NDKWCCLKSWNDBG-UHFFFAOYSA-N zinc;dioxido(dioxo)chromium Chemical compound [Zn+2].[O-][Cr]([O-])(=O)=O NDKWCCLKSWNDBG-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/83—Chemically modified polymers
- C08G18/838—Chemically modified polymers by compounds containing heteroatoms other than oxygen, halogens, nitrogen, sulfur, phosphorus or silicon
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/0091—Complexes with metal-heteroatom-bonds
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D163/00—Coating compositions based on epoxy resins; Coating compositions based on derivatives of epoxy resins
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
- C09D175/04—Polyurethanes
- C09D175/06—Polyurethanes from polyesters
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31678—Of metal
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31678—Of metal
- Y10T428/31681—Next to polyester, polyamide or polyimide [e.g., alkyd, glue, or nylon, etc.]
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31786—Of polyester [e.g., alkyd, etc.]
Definitions
- This invention is directed to a primer composition containing zircoaluminate coupling agent to improve adhesion of a waterborne base coat that has been applied to a layer of the primer.
- Zircoaluminate coupling agents have been used as adhesion promoters in adhesives and coatings to improve the adhesion of the adhesive or coating to metal substrates as shown in Claffey et al U.S. Pat. No. 4,650,526, issued Mar. 17, 1987 and Winton et al U.S. Pat. No. 5,035,940 issued Jul. 30, 1991.
- An improved solvent borne primer composition containing as the binder a polyester, polyester urethane or an epoxy polyester and a monomeric and/or polymeric alkylated melamine formaldehyde crosslinking agent and containing pigments in a pigment to binder weight ratio of about 10/100 to 200/100; where the improvement is the use of about 0.1-10% by weight, based on the weight of the binder, of a zircoaluminate coupling agent of the formula ##STR2## where R is an organo group;
- the primer provides excellent adhesion to waterborne basecoats that are applied over the primer.
- the novel primer composition of this invention has excellent adhesion to the substrate to which it is applied and provides a surface to which a waterborne base coat will adhere and not fail under end use conditions i.e. exposure to weathering, resistance to stone chipping and the like.
- a zircoaluminate couple agent to the primer composition, provides a significant improvement in adhesion of a waterborne basecoat that is applied over the primer.
- the primer composition has a film forming binder content of about 50-85% by weight and correspondingly contains about 15-50% by weight of a liquid carrier which generally is an organic solvent for the binder.
- the primer contains pigments in a pigment to binder weight ratio of about 10/100 to 200/100 and contains about 0.1-10% by weight, based on the weight of the binder, of an zircoaluminate coupling agent and preferably about 1-5% by weight of the coupling agent.
- the binder of the primer contains about 50-90% by weight of a polyester, a polyester urethane or an epoxy polyester and about 10-50% by weight of a monomeric and/or polymeric alkylated melamine formaldehyde crosslinking agent having 1-4 carbon atoms in the alkyl group.
- the polyester used in the primer is the esterification product of an alkylene glycol, a triol, and a dicarboxylic acid or anhydride or an ester of a dicarboxylic acid.
- the polyester has a number average molecular weight of about 800-10,000 and a hydroxyl no. of about 75-300 mg KOH/g polyester and an acid no. of about 2-30.
- the polyester is prepared by a conventional esterification process in which the components of the polyester are charged into a polymerization vessel with solvent and preferably with an esterification catalyst and heated to about 100°-200° C. for about 2-10 hours. Water is removed as it is formed in the process.
- Typical catalysts that can be used to form the polyester are organo tin compounds such as dibutyl tin dilaurate, dibutyl tin oxide and the like. Alkoxy titinates also are suitable catalysts.
- Typical alkylene glycols or diols that can be used to form the polyester are trimethylol pentane diol, ethylene glycol, propylene glycol, butylene glycol, neopentyl glycol, 1,6 hexane diol and the like.
- Typical triols that can be used are trimethylol propane and trimethylol ethane. Pentaerythritol also can be used.
- Aromatic dicarboxylic acids and their anhydrides that can be used are phthalic acid, phthalic anhydride, isophthalic acid, teraphthalic acid and the like.
- Hydrogenated aromatic dicarboxylic acids or their anhydrides that can be used are hexahydrophthalic acid or anhydride, tetrahydrophthalic acid or anhydride.
- Typical saturated aliphatic dicarboxylic acids or esters thereof that can be used are malonic acid, succinic acid, glutaric acid, adipic acid, pimelic acid, azelaic acid, sebacic acid, 1,4 cyclohexane dicarboxylic acid, 1,3 cyclohexane dicarboxylic acid, dimethyl 1,4 cyclohexane dicarboxylate and the like.
- Adipic acid is preferred.
- polyesters that can be used in the primer:
- Polyester urethanes can be prepared from any of the aforementioned polyesters which are reacted with an organic polyisocyanate. Any of the conventional aromatic, aliphatic, cycloaliphatic diisocyanates and trifunctional isocyanates can be used.
- diisocyanates are 1,6-hexamethlyene diisocyanate, isophorone diisocyanate, 4,4'-biphenylene diisocyanate, toluene diisocyanate, bis cyclohexyl diisocyanate, tetramethylene xylene diisocyanate, ethyl ethylene diisocyanate, 2,3-dimethyl ethylene diisocyanate, 1-methyl trimethylene diisocyanate, 1,3-cyclopentylene diisocyanate, 1,4-cyclohexylene diisocyanate, 1,3-phenylene diisocyanate, 1,5-naphthalene diisocyanate, bis -(4-isocyanatocyclohexyl)-methane, 4,4'-diisocyanatodiphenyl ether and the like.
- Typical trifunctional isocyanates that can be used are triphenylmethane triisocyanate, 1,3,5-benzene triisocyanate, 2,4,6-toluene triisocyanate and the like. Trimers of diisocyanates also can be used such as the trimer of hexamethylene diisocyanate which is sold under the tradename "Desmodur" N-3390.
- Epoxy polyesters that are useful are formed by reacting any of the aforementioned polyesters with an epoxy resin.
- Useful epoxy resins have a 1,2-epoxy equivalency of about two or more, that is, polyepoxides which have on an average basis two or more epoxy groups per molecule.
- the preferred polyepoxides are polyglycidyl ethers of cyclic polyols. Particularly preferred are polyglycidyl ethers of dihydric phenols such as bisphenol A. These polyepoxides are produced by etherification of dihydric phenols with epihalohydrin or dihalohydrin such as epichlorohydrin or dichlorohydrin in the presence of alkali.
- Epon® 828 examples of preferred commercial epoxy resins are Epon® 828, Epon® 1001, Epon® 1001F, Epon® 1002F, Epon® 1004F. Most preferred are Epon® 828 and Epon® 1001F since these resins form high quality products.
- Monomeric or polymeric alkylated melamine formaldehyde crosslinking agents or any mixtures thereof used can be partially or fully alkylated with an alkanol having 1-4 carbon atoms.
- Preferred are monomeric alkylated melamine formaldehyde crosslinking agents that are 50% butylated and 50% methylated.
- the zircoaluminate coupling agent used has the following formula ##STR3## wherein R is an organo functional group.
- R is an alkane group or an alkene group having 2-20 carbon atoms. More preferably, R is H 2 N(CH 2 ) 2 , H 3 C(CH 2 ) 12 , H 2 N(CH 2 ) 4 CH(NH 2 ), HOCH 2 CH(NH 2 ), or HSCH 2 CH(NH 2 ).
- an epoxy resin can be added to the primer to improve adhesion of the primer to an electrodeposited substrate that is applied to the steel or metal substrate typically used for autos and trucks.
- Any of the aforementioned epoxy resins can be used.
- One particularly preferred epoxy resin is Epon® 828.
- Antipoping agent and sag control agents also can be added.
- Typical pigments that can be used in the primer composition are talc, hydrophobic silica, china clay, barytes, carbonates, silicates, metallic oxides such as titanium dioxide, iron oxide, zinc oxide; carbon black, zinc chromate, and some organic colored pigment such as phthalocyanine blue and green and the like.
- the pigments generally are introduced into the primer composition by first forming a mill base with any of the aforementioned binders or with another polymer that is compatible with the binder or with a dispersing agent by conventional techniques such as sand grinding, ball milling, attritor grinding or two roll milling.
- the mill base is blended with the other constituents used to form the primer composition.
- any of the conventional solvents or blends of solvents can be used provided that the selection of solvent is such that the binder constituents are compatible and give a high quality primer.
- solvents that can be used: methanol, butanol, methyl isobutyl ketone, diisobutyl ketone, methyl ethyl ketone, methyl amyl ketone, toluene, xylene, acetone, ethylene glycol monobutyl ether acetate, butyl acetate and other ester, ethers, ketone, aliphatic and aromatic hydrocarbon solvents that are conventionally used.
- Catalysts can be added to aid in curing such as paratoluene sulfonic acid, dodecyl benzene sulfonic acid, dinonyl naphthalene disulfonic acid and the like. These catalysts can be blocked with agents such as dimethylethanolamine, aminomethyl propanol or dimethyloxazolidine.
- the primer composition can be applied by conventional techniques such as spraying, electrostatic spraying, dipping, brushing flowcoating and the like. After application, the primer is baked at an elevated temperature of about 115°-150° C. for about 10-60 minutes to form a primer layer about 10-50 microns mils thick.
- Any conventional waterborne base coats can be applied over the primer.
- these are aqueous dispersions of an acrylic polymer and an alkylated melamine formaldehyde crosslinking agent.
- Useful compositions are taught in Nickle and Werner U.S. Pat. No. 5,314,945 issued May 24, 1994 which is hereby incorporated by reference.
- Clear coating composition that can be used are shown in Harper U.S. Pat. No. 5,215,783 issued Jun. 1, 1993, Harper U.S. Pat. No. 5,227,201 issued Jul. 13, 1993 and in Lamb and Sims U.S. Pat. No. 5,286,782 issued Feb. 15, 1994 which are all incorporated herein by reference.
- clear coats of acrylic polymers and isocyanates or melamine crosslinking agents can be used.
- the base coat is applied and dried for a short period and then the clear coat is applied and both the basecoat and clear coat are cured to form a finish.
- the basecoat and clear coat are baked at about 90°-150° C. for about 10-50 minutes to fully cure these coatings.
- a primer composition was prepared by blending together the following ingredients in a suitable mixing vessel in the order shown:
- the resulting primer composition had a solids content of 73% solids and a viscosity of 65 seconds measured with #2 Ford cup.
- Two sets of zinc phosphate treated steel panels electrocoated with a standard isocyanate crosslinked epoxy resin electrocoating primer were sprayed; one set with the above prepared primer composition and the second set with primer (control) composition and each set baked at 140° C. for 30 minutes.
- the resulting primer layer was about 25 microns in thickness.
- Each of the panels was spray coated with a conventional pigmented waterborne basecoat composition of a hydroxy containing acrylic latex and a melamine crosslinking agent and baked at 121° C. for 30 minutes and tested for tape adhesion.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- General Chemical & Material Sciences (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Paints Or Removers (AREA)
Abstract
Description
______________________________________ Parts by Weight ______________________________________ Polyester resin solution (70% solids of a polyester of 994.7 TMP/NPG/AD/HHPA/THPA/PA in a weight ratio of 11/34/13/14/27/1 having a number average molecular weight of 1,600-1,700, a hydroxyl no. of 145-155 and an acid no. of 13-17 in aromatic solvent) Monomeric fully alkylated melamine formaldehyde 424.9 crosslinking agent isobutylated/methylated 50/50 ratio White pigment dispersion (64% titanium dioxide 990.0 pigment dispersed in polyester resin solution and the solvent used is a blend of butyl acetate and xylene) Carbon black pigment dispersion (8% carbon black, 107.3 polyester resin, in butyl acetate solvent) Polyester polyol (100% solids cycloaliphatic diester 152.7 diol) Zircoaluminate coupling agent having the formula 58.9 described above where R is H.sub.2 N(CH.sub.2).sub.4 CH(NH.sub.2) Methanol 55.2 Diisobutyl ketone 97.4 Dibasic ester 59.0 Dodecyl benzene sulfonic acid blocked with 2- 45.2 methyl-1-propanol "Resiflow" (10% solids of polyacrylate in xylene) 22.9 Total 3008.2 ______________________________________
TABLE ______________________________________ ADHESION TEST ASTM SAEJ400 Primer (control)/waterborne base coat - 100% adhesion failure Primer (prepared above)/waterborne basecoat - 10% adhesion failure CHIP RESISTANCEFEST ASTM D-3359-93 Primer (control) waterborne base coat/clear coat 4 Primer (prepared above) waterborne base coat/clear coat 7 Rating for chip resistance test: 10 no failure 7 passed 0 complete failure ______________________________________
Claims (8)
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/343,866 US5468791A (en) | 1994-11-17 | 1994-11-17 | Primers containing zircoaluminate coupling agents for improved adhesion |
CA002156956A CA2156956A1 (en) | 1994-11-17 | 1995-08-25 | Primers containing zircoaluminate coupling agents for improved adhesion |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/343,866 US5468791A (en) | 1994-11-17 | 1994-11-17 | Primers containing zircoaluminate coupling agents for improved adhesion |
Publications (1)
Publication Number | Publication Date |
---|---|
US5468791A true US5468791A (en) | 1995-11-21 |
Family
ID=23348024
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US08/343,866 Expired - Lifetime US5468791A (en) | 1994-11-17 | 1994-11-17 | Primers containing zircoaluminate coupling agents for improved adhesion |
Country Status (2)
Country | Link |
---|---|
US (1) | US5468791A (en) |
CA (1) | CA2156956A1 (en) |
Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0919582A1 (en) * | 1997-06-17 | 1999-06-02 | Konishi Co., Ltd. | Process for the preparation of urethane resins and urethane resin compositions |
GB2362605B (en) * | 2000-05-26 | 2004-08-25 | Becker Ind Coatings Ltd | A process of digitally printing on a substrate using an inkjettable paint, an inkjettable paint composition and a method of forming a paint composition |
US20050085569A1 (en) * | 2003-10-17 | 2005-04-21 | Yuan San C. | Chip resistant primer composition useful for producing two-tone finishes |
US20100136328A1 (en) * | 2007-02-13 | 2010-06-03 | Takayoshi Okuzu | Easy adhesion film |
US8415491B2 (en) | 2010-12-03 | 2013-04-09 | Southwest Research Institute | Surface treatment and exchange of nanostructures from aqueous suspension into organic media and into polymer-matrix composites |
US9169432B2 (en) | 2012-06-29 | 2015-10-27 | Schlumberger Technology Corporation | Spread crosslinker and method of water control downhole |
US9499733B2 (en) | 2012-06-29 | 2016-11-22 | Schlumberger Technology Corporation | Spread crosslinker and method |
US9512347B2 (en) | 2012-06-29 | 2016-12-06 | Schlumberger Technology Corporation | Spread crosslinker and method of water control downhole |
US20180118975A1 (en) * | 2014-01-15 | 2018-05-03 | Ppg Industries Ohio, Inc. | Polyester Polymers Comprising Lignin |
US9986809B2 (en) | 2013-06-28 | 2018-06-05 | The Procter & Gamble Company | Aerosol hairspray product comprising a spraying device |
CN108239510A (en) * | 2016-12-23 | 2018-07-03 | 上海轻工业研究所有限公司 | Composition of polyester hot-melt adhesive and preparation method thereof |
US10131488B2 (en) | 2015-06-01 | 2018-11-20 | The Procter And Gamble Company | Aerosol hairspray product comprising a spraying device |
US10426979B2 (en) | 2011-09-15 | 2019-10-01 | The Procter And Gamble Company | Aerosol hairspray product for styling and/or shaping hair |
US11426762B2 (en) | 2015-12-31 | 2022-08-30 | Henkel Ag & Co. Kgaa | Low bake autodeposition coatings |
US12128118B2 (en) | 2022-07-27 | 2024-10-29 | The Procter & Gamble Company | Aerosol dispenser containing a hairspray composition and a nitrogen propellant |
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1995
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Cited By (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0919582A1 (en) * | 1997-06-17 | 1999-06-02 | Konishi Co., Ltd. | Process for the preparation of urethane resins and urethane resin compositions |
US20030092867A1 (en) * | 1997-06-17 | 2003-05-15 | Shinichi Sato | Process for the preparation of urethane resins and urethane resin compositions |
EP0919582A4 (en) * | 1997-06-17 | 2004-12-29 | Konishi Co Ltd | Process for the preparation of urethane resins and urethane resin compositions |
US7208560B1 (en) | 1997-06-17 | 2007-04-24 | Konishi Co., Ltd. | Process for the preparation of urethane resins and urethane resin compositions |
US7230064B2 (en) | 1997-06-17 | 2007-06-12 | Konishi Co., Ltd. | Process for the preparation of urethane resins and urethane resin compositions |
GB2362605B (en) * | 2000-05-26 | 2004-08-25 | Becker Ind Coatings Ltd | A process of digitally printing on a substrate using an inkjettable paint, an inkjettable paint composition and a method of forming a paint composition |
US20050085569A1 (en) * | 2003-10-17 | 2005-04-21 | Yuan San C. | Chip resistant primer composition useful for producing two-tone finishes |
US7001943B2 (en) * | 2003-10-17 | 2006-02-21 | E. I. Dupont De Nemours And Company | Chip resistant primer composition useful for producing two-tone finishes |
US20100136328A1 (en) * | 2007-02-13 | 2010-06-03 | Takayoshi Okuzu | Easy adhesion film |
US8309217B2 (en) * | 2007-02-13 | 2012-11-13 | Unitika Ltd. | Easy adhesion film |
US8415491B2 (en) | 2010-12-03 | 2013-04-09 | Southwest Research Institute | Surface treatment and exchange of nanostructures from aqueous suspension into organic media and into polymer-matrix composites |
US10426979B2 (en) | 2011-09-15 | 2019-10-01 | The Procter And Gamble Company | Aerosol hairspray product for styling and/or shaping hair |
US11311749B2 (en) | 2011-09-15 | 2022-04-26 | The Procter And Gamble Company | Aerosol hairspray for styling and/or shaping hair |
US9499733B2 (en) | 2012-06-29 | 2016-11-22 | Schlumberger Technology Corporation | Spread crosslinker and method |
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